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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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ReamerPlus — 4 UDI-DI variants, MDR (QuantièmePlus SA)

MD Atlas
QuantièmePlus SA

Data from EUDAMED, last updated May 23, 2026

ReamerPlus

764016863DARCDR

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: QuantièmePlus SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 764016863DARCDR
Device name: ReamerPlus
Device model: ReamerPlus
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 7, 2023

Manufacturer & authorised representative

Manufacturer

Name: QuantièmePlus SA
SRN: CH-MF-000011186
Country: Switzerland
Email: frederic.mani@quantiemeplus.com

Authorised representative

Name: LAPE Médical
SRN: FR-AR-000007694
Country: France
Phone: +33 4899584

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01GRNNYK22XMC1NJQ441BR6QMA

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

RM0107640168630010
RM0207640168630027
RM0407640168630041
RM0307640168630034